Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Portugal-Reference-Cited by-同舟云学术

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Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Portugal

Published:2009-09 Issue:9 Volume:30 Page:1515-1517
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Bras Jose,Paisan-Ruiz Coro,Guerreiro Rita,Ribeiro Maria Helena,Morgadinho Ana,Januario Cristina,Sidransky Ellen,Oliveira Catarina,Singleton Andrew

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Clinical Neurology,Ageing,General Neuroscience

Reference7 articles.

1. Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews;Aharon-Peretz;N. Engl. J. Med.,2004

2. Gaucher disease: expression and characterization of mild and severe acid beta-glucosidase mutations in Portuguese type 1 patients;Amaral;Eur. J. Hum. Genet.,2000

3. G2019S Dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort;Bras;Movement Disord.,2005

4. Gaucher disease: N370S glucocerebrosidase gene frequency in the Portuguese population;Lacerda;Clin. Genet.,1994

5. Glucocerebrosidase mutations in subjects with parkinsonism;Lwin;Mol. Genet. Metab.,2004

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